rs1060499801

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs1060499801(C;T)

Make rs1060499801(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

77211296

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs1060499801
dbSNP (classic)	rs1060499801
ClinGen	rs1060499801
ebi	rs1060499801
HLI	rs1060499801
Exac	rs1060499801
Gnomad	rs1060499801
Varsome	rs1060499801
LitVar	rs1060499801
Map	rs1060499801
PheGenI	rs1060499801
Biobank	rs1060499801
1000 genomes	rs1060499801
hgdp	rs1060499801
ensembl	rs1060499801
geneview	rs1060499801
scholar	rs1060499801
google	rs1060499801
pharmgkb	rs1060499801
gwascentral	rs1060499801
openSNP	rs1060499801
23andMe	rs1060499801
SNPshot	rs1060499801
SNPdbe	rs1060499801
MSV3d	rs1060499801
GWAS Ctlg	rs1060499801

Max Magnitude

0

ClinVar
Risk	rs1060499801(T;T)
Alt	rs1060499801(T;T)
Reference	Rs1060499801(C;C)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	MYO7A
CLNDBN	Deafness, autosomal recessive 2
Reversed	0
HGVS	NC_000011.9:g.76922341C>T
CLNSRC
CLNACC	RCV000454216.1,